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在PCSK9抑制剂时代,我们是否需要新型降脂药物?最新进展。

Do we need new lipid-lowering agents in the era of PCSK9 inhibitors? Recent advances.

作者信息

Atar Dan, Langslet Gisle, Tonstad Serena

机构信息

Department of Cardiology, Oslo University Hospital Ulleval, Oslo, Norway.

Institute of Clinical Medicine, University of Oslo, Norway.

出版信息

Kardiol Pol. 2022;80(7-8):741-749. doi: 10.33963/KP.a2022.0117. Epub 2022 May 6.

Abstract

Atherosclerotic disease remains the leading cause of death worldwide. Much of atherosclerotic disease initiation and progression is driven by dyslipidemia. With the advent of statins, ezetimibe, and more recently the proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors, physicians across all specialties have access to an armamentarium to address this major pathophysiological driver. Nevertheless, there is still a large unmet need in terms of optimizing pharmacotherapeutic lipid lowering strategies. This article will review the evidence pertaining to the major lipid-lowering agents that have been introduced lately, or still are under development, after the advent of statins, ezetimibe and PCSK9 inhibitors. There is cumulating evidence suggesting that there soon will be a broad specter of differential therapies across a variety of mechanistic pathways that will enter clinical medicine. Knowledge about these potential recent advances and various upcoming therapeutic options will make choice easier for physicians, and will lead to more personalized selections of available treatments.

摘要

动脉粥样硬化疾病仍是全球主要死因。动脉粥样硬化疾病的发生和进展很大程度上是由血脂异常驱动的。随着他汀类药物、依折麦布以及最近的前蛋白转化酶枯草溶菌素9型(PCSK9)抑制剂的出现,各专科医生都有一系列药物可用于应对这一主要病理生理驱动因素。然而,在优化药物降脂策略方面仍有很大的未满足需求。本文将综述他汀类药物、依折麦布和PCSK9抑制剂出现后,最近引入或仍在研发的主要降脂药物的相关证据。越来越多的证据表明,很快将有一系列通过多种作用机制发挥作用的不同疗法进入临床医学。了解这些潜在的最新进展和即将出现的各种治疗选择,将使医生更容易做出选择,并能更个性化地选择现有治疗方法。

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